# Survival Benefit and Safety of Anatomic Resection in Cirrhotic Hepatocellular Carcinoma: Propensity‐Matched Analysis of 1699 Patients

**Authors:** Ao Du, Hongwei Xu, Chuang Jiang, Kefei Yuan

PMC · DOI: 10.1002/cam4.71537 · 2026-01-23

## TL;DR

Anatomic resection improves survival for liver cancer patients, including those with cirrhosis, without increasing surgical risks.

## Contribution

Demonstrates anatomic resection's survival benefit in cirrhotic and non-cirrhotic HCC patients using propensity-matched analysis.

## Key findings

- Anatomic resection improved overall and recurrence-free survival in cirrhotic HCC patients.
- Similar survival benefits were observed in non-cirrhotic HCC patients.
- No increased perioperative risks were found with anatomic resection.

## Abstract

The efficacy of anatomic resection (AR) versus non‐anatomic resection (NAR) for hepatocellular carcinoma (HCC) remains controversial, particularly among patients with differing underlying liver conditions. This study aimed to compare the outcomes of AR and NAR in HCC patients with and without liver cirrhosis.

We retrospectively analyzed data from HCC patients who underwent hepatectomy at West China Hospital between 2010 and 2022. Patients were stratified based on the presence of liver cirrhosis. Propensity score matching (PSM) was then applied separately within each stratum (cirrhotic and non‐cirrhotic) to compare perioperative outcomes and long‐term prognosis between AR and NAR.

A total of 1699 patients were enrolled, including 866 with cirrhosis and 833 without cirrhosis. Before PSM, AR was associated with significantly superior overall survival (OS) and recurrence‐free survival (RFS) compared to NAR. Following PSM (1:1 matching based on resection type within each cirrhosis stratum), similar survival advantages for AR were observed. In the matched cirrhotic cohort (255 patients per group), the AR group exhibited significantly better OS (median: 36.5 vs. 25.2 months; p < 0.001) and RFS (median: 26.9 vs. 17.4 months; p < 0.001) compared to the NAR group. Similarly, in the matched non‐cirrhotic cohort (284 patients per group), the AR group showed significantly improved OS (median: 36.3 vs. 23.9 months; p < 0.001) and RFS (median: 27.8 vs. 18.5 months; p < 0.001) compared to the NAR group. No significant differences were observed in perioperative outcomes, including postoperative complications and hospital length of stay.

Compared to NAR, AR improved long‐term prognosis in HCC patients. This survival benefit was evident even in cirrhotic patients and was not associated with increased perioperative risks.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}
- **Diseases:** hepatic injury (MESH:D056486), CCA (MESH:C536211), cardiovascular diseases (MESH:D002318), death (MESH:D003643), complication (MESH:D008107), metastasis (MESH:D009362), ICC (MESH:D018281), postoperative complication (MESH:D011183), HBV/HCV infection (MESH:D006525), diabetes (MESH:D003920), NAFLD (MESH:D065626), extrahepatic (MESH:D001651), fatty liver (MESH:D005234), MVI (MESH:D017566), varices (MESH:D014648), hypertension (MESH:D006973), splenomegaly (MESH:D013163), portal hypertension (MESH:D006975), Liver (MESH:D017093), hepatitis C virus (HCV) infection (MESH:D006526), blood loss (MESH:D016063), blood (MESH:D006402), infection (MESH:D007239), alcohol abuse (MESH:D000437), AR (MESH:D020763), postoperative hemorrhage (MESH:D019106), cirrhotic liver (MESH:D008103), hemorrhage (MESH:D006470), liver tumors (MESH:D008113), bile leakage (MESH:D003763), cancer (MESH:D009369), HCC (MESH:D006528), Cirrhosis (MESH:D005355), Cirrhotic (MESH:D000094724), HBV infection (MESH:D006509), chronic hepatitis (MESH:D006521)
- **Chemicals:** alcohol (MESH:D000438), AR (-)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Homo sapiens (human, species) [taxon 9606], hepatitis C virus [taxon 11103]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12828670/full.md

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Source: https://tomesphere.com/paper/PMC12828670